Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 9:44 PM
Ignite Modification Date:
2025-12-24 @ 9:44 PM
NCT ID:
NCT01770132
Eligibility Criteria:
Inclusion Criteria:
* Unresectable, locally advanced measurable (at least bidirectional) adenocarcinoma of the pancreas (regardless of site) proven by biopsy or cytology and confirmed by surgical consultation
* Informed consent and authorization for the release of health information signed by the patient
* Karnofsky performance status \>= 70%
* Life expectancy \>= 3 months
* Females of childbearing potential and males must use an effective method of contraception
Exclusion Criteria:
* Metastatic (stage IV) disease (including involvement of the colon, adrenals, or kidney, or radiographic evidence of peritoneal seeding or pulmonary metastases)
* Previous chemotherapy, radiotherapy of other treatment for PC
* Gastric or duodenal wall invasion by the primary PC as assessed by CT or MRI and EUS staging
* Gastric or duodenal ulcer (at least 10 mm in size) within 10 mm of expected endoscopy puncture site(s) for PDT
* Esophageal or gastric varices
* Cystic component \>= 25% the total volume of the tumor
* Ascites detected by CT, ultrasound (US) or MRI; (trace ascites will not be an exclusion)
* Bulky celiac adenopathy (i.e., \>= 2.5 cm in diameter)
* Diagnosis of islet cell tumor, lymphoma, metastatic lesion, acinar cell (or other atypical pathologic malignancy)
* History of other malignancy in the past 2 years except carcinoma in situ of the cervix or bladder, non-melanomatous skin cancer or localized/early stage prostate cancer
* Unable to receive or previously intolerant of moderate and/or deep sedation
* Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) \>= 3 x upper limit of normal (ULN)
* Total bilirubin \>= 3 x ULN
* Alkaline phosphatase \>= 3 x ULN
* International normalized ratio (INR) \>= 1.5
* Partial thromboplastin time (PTT) ratio \>= 1.5
* Serum creatinine \>= 2.0 mg/dL
* Hematocrit =\< 28% or hemoglobin =\< 9 g/dL, but may have red blood cell (RBC) transfusion
* Platelet count =\< 100,000/microliter (uL)
* Absolute neutrophil count (ANC) =\< 1500/uL
* Clinically significant pancreatitis within 12 weeks of treatment with protocol therapy
* Contraindication to EUS-guided needle puncture into the pancreas
* History of coagulopathy or known thrombophilias
* Use of anticoagulants that cannot be discontinued both 5 days before and 5 days after EUS
* Clinical evidence of active infection of any type, including hepatitis B or C virus
* Pregnant or lactating women
* Experimental medications within the last 4 weeks prior to day 1
* Any surgery (including diagnostic laparoscopy and/or biliary +/- duodenal palliative bypass for inoperable PC) within the 2 weeks prior to day 1 of study protocol
* Chronic systemic corticosteroid use at superphysiologic doses (\>= 10 mg prednisone per day or equivalent)
* Inability to avoid exposure of skin or eyes to direct sunlight or bright indoor light for at least 30 days
* Porphyria
* Inability to obtain venous access in the antecubital region to administer PHO or sedation for endoscopy procedures
* Significant concurrent medical or psychiatric illness which, in the opinion of the principal investigator would interfere with trial participation
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
60 Years
Study:
NCT01770132
Study Brief:
Protocol Section:
NCT01770132